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At least 235 records · Page 13Linked to original sources

Clinical evaluation of an automatic potassium electrode. Use of the Nova 1 ion-selective electrode in a cardiac surgical intensive care unit.

A Nova 1 potassium analyser has been evaluated for the first 3 months of its use in a cardiac surgical intensive care unit. The machine was out of action for 11 out of 104 days. 515 external calibrations were performed with 4.50 mmol/l potassium standards: mean 4.49 mmol/l, standard deviation 0.07. 692 comparisons were made with routine laboratory flame photometer measurements on the same sample: correlation coefficient r = 0.815. It is concluded that Nova 1, if kept in working order, can provide potassium estimations quickly and accurately.

Cardiac Surgical Procedures↗

A randomized comparison of a bipolar steroid-eluting electrode and a bipolar microporous platinum electrode: implications for long-term programming.

Differences in acute and chronic pacing thresholds were compared in patients receiving either the Medtronic Model 4004 steroid-eluting lead or the Medtronic Model 4012 microporous platinum lead. Patients (n = 35) were randomized at the time of implant to receive either a steroid-eluting (n = 17) or a microporous (n = 18) lead. Pacing thresholds were determined within 24 hours and at 2, 4, 6, 12, 24, and 52 weeks postimplant. By 2 weeks postimplant, pacing thresholds measured at 0.8, 1.6, 2.5, 3.3, and 4.2 V were significantly lower in the steroid lead group compared to the microporous lead group (P < 0.05). At 24 weeks, the voltage threshold at 0.3 msec was 0.8 V in 88% of patients with a steroid lead whereas this threshold was only observed in 33% of patients with the microporous lead (P < 0.01). At 52 weeks the pacing energy measured at 1.6 V, twice pulse duration threshold, was significantly lower in the steroid lead group (0.81 +/- 0.59 microJ) compared to the microporous lead group (1.25 +/- 0.60 microJ, P < 0.05). Thirteen patients in the steroid lead group and 9 patients in the microporous lead group have been programmed at a pulse amplitude of 1.6 V since the 24-week follow-up visit. These patients have been followed for a minimum of 6 months without documented failure to capture. This study shows that pacemaker/lead systems with stable chronic low thresholds can be safely programmed to low pulse amplitude settings. This practice will prolong the longevity of pulse generators.

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